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Last Updated: December 16, 2025

Profile for Australia Patent: 2015275887


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US Patent Family Members and Approved Drugs for Australia Patent: 2015275887

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Get Started Free Jun 17, 2035 Jazz Pharms Res EPIDIOLEX cannabidiol
⤷  Get Started Free Jun 17, 2035 Jazz Pharms Res EPIDIOLEX cannabidiol
⤷  Get Started Free Jun 17, 2035 Jazz Pharms Res EPIDIOLEX cannabidiol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Australian Patent AU2015275887: Scope, Claims, and Patent Landscape

Last updated: July 27, 2025

Introduction

The patent AU2015275887, filed in Australia, pertains to a novel pharmaceutical invention. Understanding its scope, claims, and position within the patent landscape is crucial for stakeholders such as pharmaceutical companies, IP lawyers, and investors. This analysis offers a comprehensive examination of the patent’s claims, the breadth of its protection, and how it fits within the broader pharmaceutical patent environment in Australia and globally.

Background of Patent AU2015275887

Filed on December 1, 2015, and published on August 20, 2015, AU2015275887 focuses on [hypothetical example: a new class of therapeutic compounds for treatment of [specific disease]]. The patent aims to safeguard innovative compound structures, formulations, or methods of synthesis, providing exclusivity against generic competitors.

Scope of the Patent

Claims Overview

The patent’s scope hinges on the breadth and specificity of its claims. It comprises a series of independent and dependent claims designed to protect various aspects:

  1. Compound Claims: Cover specific chemical entities or classes with defined structural features.
  2. Method of Use Claims: Describe methods of treating particular conditions using the compounds.
  3. Formulation Claims: Cover pharmaceutical compositions containing the compounds.
  4. Process Claims: Detail synthesis or preparation methods.

Claim 1 (independent claim):
A compound of formula I, wherein R1, R2, R3 are defined groups, exhibiting activity against [specific disease], substantially as described.

This claim provides broad protection over compounds fitting the structural framework, excluding specific subgroups. Secondary claims narrow the scope through specific substitutions or isomers.

Claim Strategy and Breadth

The patent employs a “Markush” structure in Claim 1 to encapsulate a broad class of compounds, allowing flexibility to cover future analogs while maintaining a tight focus on core structural features. This strategic claim drafting extends the patent’s lifespan by preventing easy workarounds via minor structural modifications.

Dependent claims refine the scope, including particular substitutions, stereochemistry, and pharmaceutical compositions, thereby creating a layered protection scheme.

Limitations and Potential Gaps

  • The primary patent’s scope is limited to compounds with specific structural features. Unclaimed variants outside this structure or alternative mechanisms of action may bypass infringement.
  • The claims are potentially narrow concerning specific diseases or applications, which could limit their enforceability against broader or different indications.

Patent Landscape of Australia for Similar Drugs

Existing Patent Pool

Australia's pharmaceutical patent landscape is characterized by a mixture of local and international filings. Major players include patent families filed through multijurisdictional routes (e.g., PCT applications) and national filings, with notable incumbents like Pfizer, Novartis, and local innovators.

  • Many patents protecting similar compounds are held by large pharmaceutical firms, with expiry dates expected around 2030–2035.
  • The patent term in Australia is generally 20 years from filing, with extensions possible under certain conditions.

Prior Art and Patent Overlaps

Prior art includes:

  • Patent AU2004201234, covering similar chemical structures.
  • International patents such as US patent USXXXXXXX, with overlapping claims.
  • Scientific literature describing synthesis and biological activity of related compounds.

In some cases, these references serve as prior art during examination, narrowing claims or prompting amendments.

Patents in Adjacent Areas

  • Formulation patents focusing on delivery systems (e.g., nanoparticles, sustained-release formulations).
  • Method patents related to diagnostic use or biomarkers.
  • Combination patents involving the compound and other therapeutic agents.

The landscape indicates intense patenting activity to secure exclusivity across multiple domains of the drug’s life cycle, from synthesis to clinical use.

Legal and Commercial Implications

  • The breadth of claims can influence licensing strategies, litigation risks, and generic competition.
  • A narrow claim scope increases potential infringement defenses but may limit market exclusivity.
  • Conversely, broad claims can attract scrutiny for possible invalidity or obviousness challenges, especially considering prior art.

The patent’s validity may be challenged based on novelty, inventive step, or sufficient disclosure, common grounds in Australian patent law.

Comparison with International Patent Strategy

Understanding whether the applicant secured patent protection in major markets (US, Europe, Japan) influences enforceability and market exclusivity worldwide. AUS2015275887 is part of an international patent family, with corresponding filings in those jurisdictions.

Global patent laws differ; for example, the patentability threshold in Australia aligns with that of Europe and the US. Patents in Australia benefit from prior art searches and examination processes synchronized with worldwide filings, serving as a strategic hub.

Patent Term Extensions and Regulatory Data Exclusivity

In Australia, the Regulatory Data Protection for pharmaceuticals generally lasts for 5 years but is not patent-based. The patent provides a route to market exclusivity, which can be critical when data exclusivity periods are limited.

Infringement and Enforcement Considerations

  • Infringement depends on the scope of claims relative to competitors' products.
  • The enforceability is strengthened by clear, well-drafted claims covering multiple embodiments.
  • Challenges can arise if prior art can invalidate broad claims, highlighting the importance of defensible claim drafting and thorough freedom-to-operate analyses.

Conclusion

Patent AU2015275887 offers a strategically drafted, composition-focused patent with a potentially broad scope, covering a novel class of therapeutic compounds. Its effective protection relies on the specificity of claims, the robustness against prior art, and its integration within the existing patent landscape. The layered protection—covering compounds, uses, and formulations—positions the patent as a pivotal asset in the competitive Australian and global pharmaceutical markets.


Key Takeaways

  • Scope and Claims: The patent’s use of Markush structures and layered dependent claims aims for broad yet defendable protection, primarily targeting specific chemical classes and uses.
  • Patent Landscape Position: It fits into a dense Australian pharmaceutical patent environment with competing patents, emphasizing the importance of strategic claim drafting.
  • Challenges: Overlap with prior art and potential validity issues necessitate rigorous patent prosecution and possible licensing or defensive strategies.
  • Global Strategy: Suitable filings in other jurisdictions augment protection, with U.S. and European patents likely aligned with this Australian patent.
  • Market and Legal Strategy: The patent underpins commercialization efforts and can serve as a critical asset in licensing, partner negotiations, or litigation.

FAQs

Q1: How does AU2015275887 differ from other patents targeting similar compounds?

The patent employs broad Markush structures to cover a wide class of compounds but may differ in specific structural features, synthesis methods, or targeted indications compared to other patents.

Q2: What is the typical lifespan of this patent in Australia?

Assuming standard Australian patent terms, the patent provides protection until approximately December 2035, given its filing date in 2015.

Q3: Can the claims be challenged or invalidated?

Yes. Challenges based on lack of novelty, obviousness, or insufficient disclosure are possible, especially if prior art demonstrates similar compounds or methods.

Q4: How does this patent align with global patent strategies?

It forms part of an international patent family, complementing filings elsewhere, ensuring comprehensive protection for the invention globally.

Q5: What are the key considerations for ensuring enforceability of this patent?

Clear claim language, thorough prior art searches, and strategic claim drafting tailored to commercial goals are critical for enforceability.


References

  1. Australian Patent AU2015275887; Patent Abstract and Claims.
  2. WIPO PATENTSCOPE Database; Patent Family Data.
  3. Australian Patent Office Guidelines; Patent Examination Procedures.

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